HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428979Generated: October 31, 2026
HCID 71256713, compound → HCID 71256586, compound
https://huagongshe.com/reaction/1428979
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 71256713 | HCID 71256713 | — |
| Reactant | (E)-2-(3-iodoprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 86676860 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71256586 | HCID 71256586 | — |
Reaction Steps
A reaction vial was charged with tetrabutylammonium 2-cyanobenzo[d]thiazol-6-olate (209 mg, 1.19 mmol), (E)-2-(3-iodoprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (386 mg, 1.31 mmol) and 15 mL of dry dichloromethane. The vial was sealed, and the solution was heated in an oil bath at 80° C. overnight (˜16 hours). The crude reaction mixture was added to 1 gram of celite, and the solvent was evaporated under vacuum. The product was purified by silica gel chromatography using an increasing gradient of ethyl acetate in dichloromethane as eluent. This gave 166 mg of (E)-6-((3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl)oxy)benzo[d]thiazole-2-carbonitrile as a colorless oil that crystallized to a white solid upon standing at ambient temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937183B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-60e2ec1795e04fb1959481d01f28be8c |
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| Source note | uspto-grants-2015_01 |
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